Cancer Center Jobs

Data Clinical Research Coordinator

UC Davis Comprehensive Cancer Center

December 17, 2021
The Office of Clinical Research (OCR) is a resource of the UCDHS Comprehensive Cancer Center. The overall objective of the OCR is to facilitate and coordinate cancer clinical research for Cancer Center investigators, providing investigator consultations, centralized clinical trials support for all aspects of trial management, and adherence to clinical research regulations. The OCR manages over 200 active oncology clinical trials.

Final Filing Date                      

1/6/2022

Salary Range                        

$29.16 - $46.88

We offer exceptional employment benefits including medical, dental, and vision plans, generous paid vacations and holidays, excellent retirement savings and investment plans, continuing education, and reduced fee and scholarship programs.  

THIS IS NOT AN H1- B OPPORTUNITY 

Responsibilities 

The Clinical Research Coordinator is a health professional having working knowledge of data management activities, communication skills and a willingness to cooperate as a team member. Required is the use of skills to independently or with general direction coordinate and follow through in the overall administration and outcome of clinical studies. 

Required Qualifications 

Knowledge and understanding of disease processes as applied to human clinical research.
Working knowledge of commonly used clinical trial management databases, for example, iMedidata Rave, InForm, and Oracle.
Working knowledge of Microsoft Office Suite: Word, Excel, Outlook, Access, etc.
Mathematical skills to perform calculations involving basic accounting, body surface area (BSA) calculation and drug dosage calculations.
Abstracting skills to locate relevant clinical information from medical records and other sources.
Organizational skills and attention to detail in maintaining large volumes of records, setting priorities, following through on assigned tasks and adhering to deadlines in a timely manner. 
Writing skills to compose reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms.
Demonstrate oral communication and interpersonal skills to effectively correspond with the general public, co-workers, physicians, patients, caregivers, clinic staff, and other health care professionals.
Experience working individually and as a team member in a diverse workforce.
Ability to work under the pressure of an oncology environment

Preferred Qualifications 

Previous experience coordinating oncology clinical trials 
Clinical trial coordination experience
Knowledge and understanding of oncology and disease processes as applied to clinical research.
Analytical skills to evaluate information, practices and procedures, formulate logical and objective conclusions and make recommendations for effective resolution.

Special Requirements 

This position may be subject to a criminal background investigation, drug screen, Live Scan fingerprinting, medical evaluation clearance, and functional capacity assessment.
The University of California has implemented a SARS-CoV-2 (COVID-19) Vaccination Program SARS-CoV-2 Vaccination Policy (ucop.edu) covering all employees.  To be compliant with the policy, employees must submit proof of vaccination or a University-approved exception or deferral.

EEO 

The University of California is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence.  All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.